Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H8O10S2 |
| Molecular Weight | 352.295 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC(=O)OC2=C1C=C(OS(O)(=O)=O)C(OS(O)(=O)=O)=C2
InChI
InChIKey=SZNQDPUZKFSCNG-UHFFFAOYSA-N
InChI=1S/C10H8O10S2/c1-5-2-10(11)18-7-4-9(20-22(15,16)17)8(3-6(5)7)19-21(12,13)14/h2-4H,1H3,(H,12,13,14)(H,15,16,17)
| Molecular Formula | C10H8O10S2 |
| Molecular Weight | 352.295 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Sulmarin is a water-soluble coumarin derivative with vitamin P activity. In preclinical models Sulmarin facilitates excitatory transmission from parasympathetic fibers to the gastric musculature, increasing acetylcholine release. Sulmarin reduced the tone of isolated calf coronary arteries and also inhibited the contractile response of the arteries to angiotensin II amide (Hypertensin).
Originator
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 08:59:15 GMT 2025
by
admin
on
Wed Apr 02 08:59:15 GMT 2025
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| Record UNII |
73W96524XT
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| Record Status |
Validated (UNII)
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| Record Version |
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Official Name | English | ||
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Preferred Name | English | ||
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| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C45597
Created by
admin on Wed Apr 02 08:59:15 GMT 2025 , Edited by admin on Wed Apr 02 08:59:15 GMT 2025
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| Code System | Code | Type | Description | ||
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m10384
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admin on Wed Apr 02 08:59:15 GMT 2025 , Edited by admin on Wed Apr 02 08:59:15 GMT 2025
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PRIMARY | Merck Index | ||
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CHEMBL2104898
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SUB10747MIG
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3703
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13963
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100000082952
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3573
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C74242
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249-567-8
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73W96524XT
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DTXSID10183570
Created by
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29334-07-4
Created by
admin on Wed Apr 02 08:59:15 GMT 2025 , Edited by admin on Wed Apr 02 08:59:15 GMT 2025
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| Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
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ACTIVE MOIETY |